Method of manufacturing composite products comprising a carbohydrate-based binder

ABSTRACT

The present invention relates to the use of an amine compound comprising at least one, preferably at least two amine functions, wherein the amine functions are primary or secondary amines, to reduce the level of furfural and/or hydroxymethylfurfural in a carbohydrate-based binder or binder composition and/or escaping in the course of preparation, cross-linking and/or curing of carbohydrate-based binders. Preferably, the carbohydrate-based binder is obtained from a carbohydrate-based binder composition comprising a carbohydrate component and a cross-linker and possibly reaction product of carbohydrate component and cross-linker, wherein the cross-linker is selected from ammonium salts of inorganic acid, carboxylic acids, salts, ester or anhydride derivatives thereof, and/or combinations thereof.

The present invention relates to a method of manufacturing composite products, more specifically composite products comprising fibers, particles, chips, strips, and/or sheets bonded with a binder. Examples of such composite products include woven and non-woven fiber mats, such as mineral fiber mats, for example mineral wool mats (glass wool, rock wool), mineral fiber veils, prepregs, engineered wood products, such as wood boards, for example MDF (Medium Density Fiber Boards), particle boards, oriented strand boards (OSB), plywood etc.

The trend to more sustainable and environmentally friendly products has directed the development of such composite products away from the use of formaldehyde based binders towards the use of formaldehyde-free binders. Among such formaldehyde-free binders, carbohydrate-based binders represent an important share.

In the context of this description, “formaldehyde-free” is understood to mean “comprising less than about 1 ppm formaldehyde based on the weight of the composition and not liberating substantial formaldehyde”.

Carbohydrate based binders include binders obtained by the reaction of a carbohydrate with a nitrogenous compound, such as Maillard-type binders, by the reaction of a carbohydrate with an organic acid, and other binders obtained from starting materials that include a carbohydrate.

Carbohydrates are readily available in nature. Sources are animal derived products such as chitosan (derived from crustacean shells) and plant derived products, including but not limited to starch, syrup, molasses and cellulose. These carbohydrates also called polysaccharides are macromolecules made up by saccharide units. An advantageous source of carbohydrate raw materials can be found in recycled materials, such as recycled municipal solid waste, recycled paper and/or sugar cane bagasse, and/or wood. Depending on the source and/or on the hydrolysis process used to degrade the polysaccharides, different polysaccharides or polysaccharide compositions may be obtained. In certain applications, smaller molecules may be preferred, such as short chain polysaccharides, oligosaccharides or even saccharide units. Again, depending on the source and/or hydrolysis process conditions, different saccharides or saccharide mixtures may be obtained. While cellulose hydrolysis will generate essentially C6 sugars, preferably C-6 reducing sugars, e.g. dextrose, hemicellulose will generate a large fraction of C5 sugars, like xylose for instance.

In raw materials resulting from hydrolysis of higher molecular weight carbohydrates, the level of C5-sugars or five membered ring sugars has been found to vary from 5 to 70 wt. %, preferably from 10, from 15, from 20 or even from 25% by weight, and up to preferably 60 wt. %, 50 wt. %, 45 wt. % or 40 wt. %.

It is known that saccharides may give rise to furfural and/or hydroxymethylfurfural formation in the course of the binder preparation and/or binder curing process. While starting from raw materials as discussed above to produce a binder may be of interest for several reasons, such as the availability of raw materials and costs of the manufacturing process, it has been found that the presence of C-5 sugars in the carbohydrate component gives rise to increased furfural and/or hydroxymethylfurfural generation in the course of the binder preparation and/or curing process. Furfural and/or hydroxymethylfurfural may be undesirable beyond a certain level, for environmental and/or health reasons, but also because of regulatory requirements. There is thus a need to reduce the level of furfural and/or hydroxymethylfurfural generated in the course of binder preparation and/or curing.

It has now been found that the level of furfural and/or hydroxymethylfurfural in the binder composition and/or escaping during binder preparation and/or curing may be reduced by addition of an amine compound, preferably an amine compound comprising at least one, preferably at least two amine functions, wherein the amine functions are primary or secondary amines.

The present invention hence provides a method for the preparation of a composite product comprising fibers and/or particles and/or sheet material bonded with a carbohydrate-based binder comprising (i) providing a binder composition comprising a carbohydrate component and a cross-linker and possibly reaction product of carbohydrate component and cross-linker, wherein the cross-linker is selected from ammonium salts of inorganic acid, carboxylic acids, salts, for example ammonium salts thereof, ester or anhydride derivatives thereof, and/or combinations thereof, (ii) adding to the binder composition an additional amount of from 0.5 to 10 wt. %, preferably 1 to 6 wt. % (based on the total dry weight of the binder composition) of an amine compound comprising at least one, preferably at least two amine functions, wherein the amine functions are primary or secondary amines, (iii) applying the composition obtained under (ii) onto the fibers, particles and/or sheet material, and (iv) subjecting the product obtained under (iii) to heat and possibly pressure to effect drying and/or curing.

As used herein, “ammonium” means NH₄ ⁺.

The term “binder composition” as used herein means all ingredients applied to the matter to be bound and/or present on the matter to be bound, notably prior to curing, (other than the matter and any moisture contained within the matter) including reactants, solvents (including water), any carbohydrate component, any crosslinker and any additives.

The term “binder” is used herein to designate a thermoset binder resin obtained from the “binder composition”.

The term “cured” means that the components of the binder composition have been subjected to conditions that lead to chemical change, such as covalent bonding, hydrogen bonding and chemical crosslinking, which may increase the cured product's durability and solvent resistance, and result in thermoset material.

The term “dry weight of the binder composition” as used herein means the weight of all components of the binder composition other than any water that is present (whether in the form of liquid water or in the form of water of crystallization).

The term “crosslinker” as used herein comprises compounds that are capable of reacting with the carbohydrate component to form ramifications or reticulations of the said carbohydrate component. As is understood, the cross-linker is different from and does not comprise any amine compound as defined above.

Carbohydrates as used herein comprise monosaccharides, disaccharides, oligosaccharides and polysaccharides and/or combinations thereof. They may be reducing sugars, such as dextrose, or non-reducing sugars, such as sucrose, that may produce reducing sugars in situ. They may advantageously be a low MW polysaccharide. In one embodiment, the carbohydrate component may be selected from or derived from molasses, starch, starch hydrolysates, dextrines and derivatives, cellulose hydrolysates, hemicellulose hydrolysates or mixtures thereof. As mentioned before, the carbohydrate component may be obtained from animal derived material and/or plant derived material. In a preferred embodiment, the carbohydrate component is derived from higher molecular weight carbohydrates, wherein the level of C5-sugars or five membered ring sugars varies from 10 to 70 wt. %, preferably from 15, from 20 or even from 25% by weight, and up to preferably 60 wt. %, 50 wt. %, 45 wt. % or 40 wt. %.

Suitable amine compounds comprise at least one, preferably at least two amine functions, wherein the amine functions are primary or secondary amines, the amine compound comprising preferably at least one primary amine function. The amine compound is advantageously selected from aliphatic monoamines, wherein the aliphatic group is a straight or branched saturated or unsaturated alkyl or hetero-alkyl chain having 2 to 24 C-atoms or cycloalkyl or cyclohetero-alkyl or an aromatic carbon ring structure, each possibly substituted by hydroxy, carboxyl, halo, cyanate, sulfonyl or thiol, from compounds of general formula H₂N-Q-NH₂ wherein Q is a straight or branched alkanediyl, heteroalkanediyl having 2 to 24 C-atoms, cycloalkanediyl, or cylcoheteroalkanediyl, an aromatic carbon ring structure, possibly substituted by hydroxy, carboxyl, halo, cyanate, sulfonyl and/or thiol, or from proteins, such as whey or soy protein, possibly modified or denatured, or from poly(primary amines) having a molecular weight of 5000 or less and 10 wt. % or more of primary amine groups based on the weight of the polyamine. According to a preferred embodiment, Q is a C₆ alkanediyl. According to another embodiment, Q may be a cyclohexanediyl, cyclopentanediyl or cyclobutanediyl, or a divalent benzyl radical. In this context, it should be noted that certain authors prefer using the term “alkyl” instead of the chemically more correct “alkanediyl” nomenclature; the same chemical group is meant. As used herein, the term “alkanediyl” means a chain of carbon atoms, which may optionally be branched, preferably of limited length, including —C₁-C₂₄—, —C₁-C₁₂—, —C₁-C₈—, —C₁-C₆—, and —C₁-C₄—. Shorter alkanediyl groups may add less lipophilicity to the compound and accordingly will have different reactivity towards the reducing sugar reactant and/or solubility. As used herein, the term “cycloalkanediyl” means a chain of carbon atoms, which may optionally be branched, where at least a portion of the chain is cyclic and also includes polycyclic structures, for example, cyclopropanediyl, cyclopentanediyl, cyclohexanediyl, 2-methylcyclopropanediyl, 2-ethylcyclopentanediyl, adamantanediyl. Furthermore, the chain forming cycloalkanediyl is advantageously of limited length, including —C₃-C₂₄—, —C₃-C₁₂—, —C₃-C₈—, —C₃-C₆—, and —C₅- C₆—. Shorter alkanediyl chains forming cycloalkanediyl may add less lipophilicity to the compound and accordingly will have a different behaviour.

The poly(primary amine) may be selected from polyetheramines, polyethyleneimines, polyethyleneimine containing copolymers and block copolymers, polyvinyl amines, (co)polymers of n-aminoalkyl (meth)acrylates, such as aminoethyl methacrylate.

In illustrative embodiments, the polyamine is selected from a group consisting of a diamine, triamine, tetraamine, and pentamine. In one embodiment, the polyamine is a diamine selected from a group consisting of 1,6-diaminohexane and 1,5-diamino-2-methylpentane. In one embodiment, the diamine is 1,6-diaminohexane. In one embodiment, the polyamine is a triamine selected from a group consisting of diethylenetriamine, 1-piperazineethaneamine, and bis(hexamethylene)triamine. In another embodiment, the polyamine is a tetramine such as triethylenetetramine. In another embodiment, the polyamine is a pentamine, such as tetraethylenepentamine.

The relevant amine compound may also be selected from aminoacids. Some are primary monoamines; others are di-primary amines. Lysine is an example of a diamine which has shown to perform well and which is readily available for applications under consideration.

Another amine compound family that has shown to perform well are urea based compounds, more particularly urea. Urea comprises two-NH₂ groups which are available for reaction.

As used herein the term “carboxylic acid” includes monocarboxylic acids as well as polycarboxylic acids, salts, ester and anhydride derivatives thereof. The term “polycarboxylic acid” indicates a dicarboxylic, tricarboxylic, tetracarboxylic, pentacarboxylic, and monomeric polycarboxylic acids, as well as polymeric polycarboxylic acids, and combinations thereof. In one aspect, the polycarboxylic acid ammonium salt reactant is sufficiently non-volatile to maximize its ability to remain available for reaction with the carbohydrate reactant of a Maillard reaction (discussed below). In another aspect, the polycarboxylic acid ammonium salt reactant may be substituted with other chemical functional groups. Monomeric polycarboxylic acid comprises dicarboxylic acid, including, but not limited to, unsaturated aliphatic dicarboxylic acids, saturated aliphatic dicarboxylic acids, aromatic dicarboxylic acids, unsaturated cyclic dicarboxylic acids, saturated cyclic dicarboxylic acids, hydroxy-substituted derivatives thereof, and the like. Polycarboxylic acid(s) may be a tricarboxylic acid, including, but not limited to, unsaturated aliphatic tricarboxylic acids, saturated aliphatic tricarboxylic acids, aromatic tricarboxylic acids, unsaturated cyclic tricarboxylic acids, saturated cyclic tricarboxylic acids, hydroxy-substituted derivatives thereof, and the like. It is appreciated that any such polycarboxylic acids may be optionally substituted, such as with hydroxy, halo, alkyl, alkoxy, and the like. In one variation, the polycarboxylic acid is the saturated aliphatic tricarboxylic acid, citric acid. Other suitable polycarboxylic acids are contemplated to include, but are not limited to, aconitic acid, adipic acid, azelaic acid, butane tetracarboxylic acid dihydride, butane tricarboxylic acid, chlorendic acid, citraconic acid, dicyclopentadiene-maleic acid adducts, diethylenetriamine pentaacetic acid, adducts of dipentene and maleic acid, ethylenediamine tetraacetic acid (EDTA), fully maleated rosin, maleated tall-oil fatty acids, fumaric acid, glutaric acid, isophthalic acid, itaconic acid, maleated rosin oxidized with potassium peroxide to alcohol then carboxylic acid, maleic acid, malic acid, mesaconic acid, biphenol A or bisphenol F reacted via the KOLBE-Schmidt reaction with carbon dioxide to introduce 3-4 carboxyl groups, oxalic acid, phthalic acid, sebacic acid, succinic acid, tartaric acid, terephthalic acid, tetrabromophthalic acid, tetrachlorophthalic acid, tetrahydrophthalic acid, trimellitic acid, trimesic acid, and the like, and anhydrides, and combinations thereof.

Illustratively, a polymeric polycarboxylic acid may be an acid, for example, polyacrylic acid, polymethacrylic acid, polymaleic acid, and like polymeric polycarboxylic acids, copolymers thereof, anhydrides thereof, and mixtures thereof. Examples of commercially available polyacrylic acids include AQUASET-529 (Rohm & Haas, Philadelphia, PA, USA), CRITERION 2000 (Kemira, Helsinki, Finland, Europe), NF1 (H.B. Fuller, St. Paul, MN, USA), and SOKALAN (BASF, Ludwigshafen, Germany, Europe). With respect to SOKALAN, this is a water-soluble polyacrylic copolymer of acrylic acid and maleic acid, having a molecular weight of approximately 4000. AQUASET-529 is a composition containing polyacrylic acid cross-linked with glycerol, also containing sodium hypophosphite as a catalyst. CRITERION 2000 is an acidic solution of a partial salt of polyacrylic acid, having a molecular weight of approximately 2000. With respect to NF1, this is a copolymer containing carboxylic acid functionality and hydroxy functionality, as well as units with neither functionality; NF1 also contains chain transfer agents, such as sodium hypophosphite or organophosphate catalysts.

Further, compositions including polymeric polycarboxylic acids are also contemplated to be useful in preparing the binders described herein, such as those compositions described in U.S. Pat. Nos. 5,318,990, 5,661,213, 6,136,916, and 6,331,350, the disclosures of which are hereby incorporated herein by reference. In particular, in U.S. Pat. Nos. 5,318,990 and 6,331,350, an aqueous solution of a polymeric polycarboxylic acid, a polyol, and a catalyst is described. As described in U.S. Pat. Nos. 5,318,990 and 6,331,350, the polymeric polycarboxylic acid comprises an organic polymer or oligomer containing more than one pendant carboxy group. The polymeric polycarboxylic acid may be a homopolymer or copolymer prepared from unsaturated carboxylic acids including, but not necessarily limited to, acrylic acid, methacrylic acid, crotonic acid, isocrotonic acid, maleic acid, cinnamic acid, 2-methylmaleic acid, itaconic acid, 2-methylitaconic acid, α,β-methyleneglutaric acid, and the like. Alternatively, the polymeric polycarboxylic acid may be prepared from unsaturated anhydrides including, but not necessarily limited to, maleic anhydride, itaconic anhydride, acrylic anhydride, methacrylic anhydride, and the like, as well as mixtures thereof. Methods for polymerizing these acids and anhydrides are well-known in the chemical art. The polymeric polycarboxylic acid may additionally comprise a copolymer of one or more of the aforementioned unsaturated carboxylic acids or anhydrides and one or more vinyl compounds including, but not necessarily limited to, styrene, α-methylstyrene, acrylonitrile, methacrylonitrile, methyl acrylate, ethyl acrylate, n-butyl acrylate, isobutyl acrylate, methyl methacrylate, n-butyl methacrylate, isobutyl methacrylate, glycidyl methacrylate, vinyl methyl ether, vinyl acetate, and the like. Methods for preparing these copolymers are well-known in the art. The polymeric polycarboxylic acids may comprise homopolymers and copolymers of polyacrylic acid. The molecular weight of the polymeric polycarboxylic acid, and in particular polyacrylic acid polymer, may be less than 10000, less than 5000, or about 3000 or less. For example, the molecular weight may be 2000.

Preferred cross-linkers are selected from ammonium salts of inorganic acids, such as ammonium sulphate or ammonium phosphate, and ammonium salts of carboxylic acids. Further suitable cross-linkers are salt, ester and anhydride derivatives of carboxylic acids, preferably polycarboxylic acids, more preferably monomeric polycarboxylic acids.

In a further aspect, the present invention relates to a composite material obtained by the method of the invention, the said composite material comprising a reduced furfural and/or hydroxymethylfurfural content as compared with a composite material obtained from the same raw material transformed under the same processing conditions but with no added amine compound comprising at least one, preferably at least two amine functions, wherein the amine functions are primary or secondary amines.

The binder composition may be used in the manufacturing of composite products, such as wood boards, for example wood particle boards, medium density fibreboard (MDF), chip boards or orientated strand board (OSB), and plywood. The binder may be used to bond abrasive particles together and/or onto a backing sheet or to bond fibers, such as woven and non-woven natural, synthetic, textile or mineral fibers, for instance glass fibers or mineral wool fibers. Such bonded mineral fibers, for instance mineral glass wool or stone wool fibers, may be used in the manufacturing of thermal and/or acoustic insulating materials.

A wood particle board is a composite material manufactured from wood particles, for example wood chips, sawmill shavings and/or saw dust at varying particle sizes held together by a binder and used especially for the manufacture of furniture, such as cabinets, kitchens and bathroom furniture. Generally, wood particle board (which is sometimes referred to as “chipboard”) is produced by mixing wood particles and a binder composition, e.g. a thermo-curable resin, subsequently forming the resulting mixture into a sheet or mat and compressing said sheet or mat under elevated temperatures.

Plywood is a composite sheet material manufactured from thin layers of wood glued together by a binder, adjacent wood layers having their wood grain rotated by approx. 90 degrees to one another.

When used as a binder in wood boards, such as plywood, particle boards, fiber boards, the solid content of the aqueous binder composition may range from 50 to 95 w %, preferably 50 to 90 w %, more preferably 55 to 85 w % or even 60 to 80 w %, based upon the weight of the total aqueous binder composition.

The binder may also be used to bond synthetic or natural fibers, for instance mineral fibers, such as glass fibers, glass wool or stone wool. In view of the manufacture of a fiber mat, such as for insulating products, for instance, an aqueous binder composition is applied onto the fibers, e.g. by spraying, and the binder impregnated mineral fibers are deposited as a mat and subsequently subjected to heat for curing of the binder composition, hence forming an assembly of bonded fibers.

When used in the manufacture of a fiber based composite, the solid content of the invention aqueous binder composition may range from 5 to 95 w %, advantageously from 8 to 90 w %, preferably from 10 to 85 w %, based on the weight of the total aqueous binder composition. More specifically, when used as a binder for mineral wool insulation, the solid content of the aqueous binder composition may be in the range from 5 to 25 w %, preferably from 8 to 20 w %, more preferably from 10 to 20 w % or even 12 to 18 w %, based on the weight of the total aqueous binder composition.

In the binder composition, the carbohydrate component is advantageously present in an amount ranging from 30%, preferably from 40%, preferably from 50%, more preferably from 60%, more preferably from 70%, even more preferably from 80% by dry weight of the binder composition, to less than 97% more preferably less than 95% by dry weight of the binder composition.

The crosslinker may make up:

less than 50% or 40%, preferably less than 30%, more preferably less than 25% by dry weight of the binder composition; and/or

at least 2.5%, preferably at least 5%, more preferably at least 10% by dry weight of the binder composition.

The binder composition may comprise at least 25%, and preferably at least 40%, at least 50% or at least 60% by dry weight of: (a) carbohydrate component and crosslinker and/or (b) curable reaction product(s) of carbohydrate component and crosslinker.

The crosslinker and the carbohydrate component (or their reaction product(s)) may be Maillard reactants that react to form Maillard reaction products, notably melanoidins when cured. Curing of the binder composition may comprise or consist essentially of Maillard reaction(s). The cured binder is preferably a thermoset binder and is preferably substantially water insoluble.

The binder composition may further comprise one or more adjuvants, for example waxes, dyes, release agents, formaldehyde scavengers, hydrophobizing agents and other adjuvants commonly used in binder compositions. In certain applications, such as for example the bonding of mineral fibers, coupling agents, such as for example silicon-based coupling agents may advantageously be combined with the binder components in the binder composition. Also, catalysts, such as mineral phosphorous-based salts and/or acids, such as phosphate or hypophosphite salts, may be added into the binder composition as catalysts of the resin forming reaction.

Further advantages of the invention will become apparent from the Examples herein below.

FIG. 1 is a chart showing the variation of furfural content in a binder derived from a carbohydrate component comprising dextrose and xylose in varying amounts, cross-linked with ammonium sulphate, as well as the effect of added hexamethylenediamine.

EXAMPLE 1

Dextrose and varying amounts of xylose were dissolved in water to constitute different carbohydrate components. These carbohydrate components were combined with ammonium sulphate cross-linker (AMS) to form aqueous binder compositions at a dry weight ratio of carbohydrate/AMS of 85/15 and at 37.5 wt. % solids. The same procedure was repeated with binder compositions as above further comprising 2 and 4 wt. % hexamethylene diamine. GFA glass filters were impregnated with the relevant binders at a rate of 15% by weight cured solids, and cured during 5 min at 180° C.

The furfural concentration of the cured binder was determined by leaching the impregnated filter into a small quantity of water at room temperature for 1 hour and analysing the leachate for furfural and hydroxyfurfural by HPLC (C18 column, acetonitrile/water mobile phase, UV detector). The results were plotted in a chart as per FIG. 1 which clearly shows that addition of small amounts of hexamethylene diamine significantly depresses furfural generation.

EXAMPLE 2

The same experiment as above was repeated for the compositions shown in the Tables below, in comparison with corresponding compositions containing no amine.

As can be understood, added urea, lysine and some further polyamines efficiently reduce furfural concentration in the leachate.

TABLE 1 Furfural reduction in 85/15 glucose/(NH₄)₂SO₄ binder compositions % Reduction in % Reduction in Amine Furfural + 2% amine Furfural + 4% amine HMDA  8% 95% Lupasol FG  9% 48% Urea 36% 47% TETA 16% 46% Triethylenetetramine Lysine  7% 22% Luredur VM  0% 16% Ethylamine  0%  0% Jeffamine T-403  0%  0%

TABLE 2 Furfural reduction in 85/15 sugar/(NH₄)₂SO₄ binder compositions, wherein the sugar composition comprises 60% wt. glucose and 40% wt. xylose. % Reduction in % Reduction in Furfural + 2 % Furfural + 4% Amine amine amine HMDA 27% 98% Lysine 16% 29% TETA 15% 26% Triethylenetetramine Lupasol FG  6% 23% Urea 12% 22% Jeffamine T-403  9% 19% Ethylamine  2% 18% Luredur VM  0%  6%

In the Tables above, HMDA stands for hexamethylenediamine Lupasol FG (commercial name) is a polyethylenimine Jeffamine T-403 (commercial name) is a polyetheramine Luredur VM (commercial name) is a polyvinylamine 

What is claimed is: 1-24. (canceled)
 25. A method for the preparation of a composite product comprising one or more fibers, particles sheet materials and/or combinations thereof bonded with a carbohydrate-based binder comprising (i) providing a binder composition comprising a carbohydrate component, a cross-linker component and optionally one or more reaction products of the carbohydrate component and the cross-linker component, wherein the cross-linker component is selected from the group consisting of ammonium salts, inorganic acids, carboxylic acids, ester and/or anhydride derivatives thereof, and/or combinations thereof; (ii) adding 0.5-10% by weight (wt. %, based on the total dry weight of the binder composition) of a urea comprising compound to the binder composition; (iii) applying the binder composition produced in step (ii) to the one or more fibers, particles sheet materials and/or combinations thereof for forming the composite product; and (iv) applying heat and/or pressure to dry and/or cure the composite product.
 26. The method of claim 25, wherein the cross-linker component is selected from the group consisting of an ammonium salt of an inorganic acid, ammonium sulfate, ammonium phosphate and combinations thereof.
 27. The method of claim 25, wherein the cross-linker component is selected from the group consisting of a carboxylic acid, an ammonium salts thereof, an ester derivative thereof, an anhydride derivative thereof, a polycarboxylic acid, a monomeric polycarboxylic acid and combinations thereof.
 28. The method of claim 25, wherein the carbohydrate component is selected from the group consisting of a monosaccharide, a disaccharide, an oligosaccharide, a polysaccharide, a reducing sugar, dextrose, a non-reducing sugar, sucrose, reducing sugars produced in situ, derivatives thereof and combinations thereof.
 29. The method of claim 25, wherein the carbohydrate component is selected from the group consisting of a low molecular weight (MW) polysaccharide, molasses, starch, a starch hydrolysate, dextrin, a cellulose hydrolysate, a hemicellulose hydrolysate, derivatives thereof and combinations thereof.
 30. The method of claim 25, wherein the carbohydrate component comprises one or more higher molecular weight carbohydrate derivatives comprising 10-70 wt. % C5 sugars and/or five-membered ring sugars.
 31. The method of claim 25, wherein the carbohydrate component comprises 30-97% by dry weight of the binder composition.
 32. The method of claim 25, wherein the cross-linker component comprises 10-25% by dry weight of the binder composition.
 33. The method of claim 25, wherein the binder composition produced in step (ii) is characterized by reduced concentrations of furfural and/or hydroxymethylfurfural as compared to a binder composition not produced in accordance with step (ii).
 34. The method of claim 25, wherein the binder composition produced in step (ii) is characterized by reduced levels of furfural and/or hydroxymethylfurfural emission as compared to a binder composition not produced in accordance with step (ii).
 35. The method of claim 25, wherein the binder composition further comprises one or more adjuvants, waxes, dyes, release agents, formaldehyde scavengers, hydrophobizing agents, silicon-based coupling agents, phosphorous comprising salts, phosphorous comprising acids, phosphate salts, hypophosphite salts and combinations thereof.
 36. The method of claim 25, wherein the composite product is selected from the group consisting of a wood board, a wood particle board, a fiberboard, a medium density fiberboard (MDF), a chip board, an orientated strand board (OSB), plywood, a glass fiber product, a glass wool product, a mineral wool fiber product, a thermal insulating material product and an acoustic insulating material product.
 37. A method for reducing furfural and/or hydroxymethylfurfural concentrations and/or emissions in a binder composition comprising a carbohydrate component and a cross-linker comprising (i) preparing a binder composition reaction medium comprising a carbohydrate component, a cross-linker component and optionally one or more reaction products of the carbohydrate component and the cross-linker component; and (ii) adding a urea comprising compound to the binder composition reaction medium of step (i) to form the binder composition; wherein the reduced furfural and/or hydroxymethylfurfural concentrations and/or emissions are determinable during the preparation, cross-linking and/or curing of the binder composition; and wherein the reduced furfural and/or hydroxymethylfurfural concentrations and/or emissions are determined in comparison to a binder composition not produced in accordance with step (ii).
 38. The method of claim 37, wherein the cross-linker component is selected from the group consisting of ammonium salts, inorganic acids, carboxylic acids, ester and/or anhydride derivatives thereof, ammonium sulfate, ammonium phosphate and/or combinations thereof.
 39. The method of claim 37, wherein the urea comprising compound is added at a concentration of 0.5-10 wt. %, based on the total dry weight of the binder composition.
 40. The method of claim 37, wherein the carbohydrate component comprises 30-97% by dry weight of the binder composition.
 41. The method of claim 37, wherein the carbohydrate component comprises one or more higher molecular weight carbohydrate derivatives comprising 10-70 wt. % C5 sugars and/or five-membered ring sugars.
 42. A composite product produced by the method of claim
 25. 43. The composite product of claim 42, comprising reduced concentrations of furfural and/or hydroxymethylfurfural as compared to a composite material not produced by the method of claim
 25. 44. The composite product of claim 42, wherein the composite product is characterized by reduced levels of furfural and/or hydroxymethylfurfural emission as compared to a composite material not produced by the method of claim
 25. 